manual: quikchange xl site-directed mutatgenesis kit

Manual: QuikChange XL Site-Directed Mutatgenesis KitInstruction Manual
Catalog # 200516 (30 reactions) and 200517 (10 reactions) Revision D
Research Use Only. Not for Use in Diagnostic Procedures. 200516-12
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QuikChange XL Site-Directed Mutagenesis Kit
CONTENTS Materials Provided.............................................................................................................................. 1 Storage Conditions.............................................................................................................................. 1 Additional Materials Required .......................................................................................................... 1 Notice to purchaser ............................................................................................................................. 2 Introduction......................................................................................................................................... 3 QuikChange XL Mutagenesis Control.............................................................................................. 5 Mutagenic Primer Design................................................................................................................... 6
QuikSolution ......................................................................................................................... 9 Mutant Strand Synthesis Reaction (Thermal Cycling).......................................................... 9 Dpn I Digestion of the Amplification Products................................................................... 11 Transformation of XL10-Gold Ultracompetent Cells ......................................................... 11
Transformation Guidelines .............................................................................................................. 14 Storage Conditions .............................................................................................................. 14 Aliquoting Cells .................................................................................................................. 14 Use of 14-ml BD Falcon Polypropylene Round-Bottom Tubes.......................................... 14 Use of β-Mercaptoethanol ................................................................................................... 14 Quantity of DNA Added ..................................................................................................... 14 Length and Temperature of the Heat Pulse ......................................................................... 14 Preparing the Agar Plates for Color Screening ................................................................... 14
Troubleshooting ................................................................................................................................ 15 Preparation of Media and Reagents ................................................................................................ 16 References .......................................................................................................................................... 17 Endnotes............................................................................................................................................. 17 MSDS Information............................................................................................................................ 17
QuikChange XL Site-Directed Mutagenesis Kit
MATERIALS PROVIDED Quantity
10× reaction bufferc 500 μl 500 μl
Dpn I restriction enzyme (10 U/μl) 300 U 100 U
Oligonucleotide control primer #1 [34-mer (100 ng/μl)]
5´ CCA TGA TTA CGC CAA GCG CGC AAT TAA CCC TCA C 3´
750 ng 750 ng
Oligonucleotide control primer #2 [34-mer (100 ng/μl)]
5´ GTG AGG GTT AAT TGC GCG CTT GGC GTA ATC ATG G 3´
750 ng 750 ng
pWhitescript 4.5-kb control plasmid (5 ng/ μl) 50 ng 50 ng
QuikSolution 500 μl 500 μl
dNTP mixd,e 30 μl 10 μl
XL10-Gold ultracompetent cellsf (yellow tubes) 10 × 135 μl 4 × 135 μl
XL10-Gold β-mercaptoethanol mix (β-ME) 2 × 50 μl 50 μl
pUC18 control plasmid (0.1 ng/μl in TE bufferc) 10 μl 10 μl a The QuikChange XL Site-Directed Mutagenesis Kit (Catalog #200516) contains enough reagents for 30 total reactions,
which includes 5 control reactions. b The QuikChange XL Site-Directed Mutagenesis Kit (Catalog #200517) contains enough reagents for 10 total reactions,
which includes 5 control reactions. c See Preparation of Media and Reagents. d Thaw the dNTP mix once, prepare single-use aliquots, and store the aliquots at –20°C. Do not subject the dNTP mix
to multiple freeze-thaw cycles. e The composition of the dNTP mix is proprietary. This reagent has been optimized for the QuikChange XL site-
directed mutagenesis protocols and has been qualified for use in conjunction with the other kit components. Do not substitute with dNTP mixes provided with other Stratagene kits.
f Genotype: TetrΔ (mcrA)183 Δ(mcrCB-hsdSMR-mrr)173 endA1 supE44 thi-1 recA1 gyrA96 relA1 lac Hte [F’ proAB lacIqZΔM15 Tn10 (Tetr) Amy Camr]
STORAGE CONDITIONS XL10-Gold Ultracompetent cells, XL10-Gold β-ME, and pUC18 Control Plasmid: –80°C All Other Components: –20°C
ADDITIONAL MATERIALS REQUIRED 14-ml BD Falcon polypropylene round-bottom tubes (BD Biosciences Catalog #352059) 5-Bromo-4-chloro-3-indloyl-β-D-galactopyranoside (X-gal) Isopropyl-1-thio-β-D-galactopyranoside (IPTG)
Revision D © Agilent Technologies, Inc. 2010.
2 QuikChange XL Site-Directed Mutagenesis Kit
NOTICE TO PURCHASER
Notice to Purchaser: Limited License Purchase of this product includes an immunity from suit under patents specified in the product insert to use only the amount purchased for the purchaser’s own internal research. No other patent rights (such as 5’ Nuclease Process patent rights) are conveyed expressly, by implication, or by estoppel. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.
QuikChange XL Site-Directed Mutagenesis Kit 3
INTRODUCTION In vitro site-directed mutagenesis is an invaluable technique for studying protein structure-function relationships and gene expression, and for carrying out vector modification. Several approaches to this technique have been published, but these methods generally require single-stranded DNA (ssDNA) as the template1-4 and are labor intensive or technically difficult. The QuikChange XL Site-Directed Mutagenesis Kit* allows site-specific mutation in virtually any double-stranded plasmid, thus eliminating the need for subcloning into M13-based bacteriophage vectors and for ssDNA rescue.5 In addition, the QuikChange XL system requires no specialized vectors, unique restriction sites, or multiple transformations. This rapid four- step procedure generates mutants with greater than 80% efficiency. The protocol is simple and uses either miniprep plasmid DNA or cesium-chloride-purified DNA. The QuikChange XL system is used to make point mutations, switch amino acids, and delete or insert single or multiple amino acids. The QuikChange XL method is performed using PfuTurbo DNA Polymerase** and a thermal temperature cycler. PfuTurbo DNA polymerase replicates both plasmid strands with high fidelityll and without displacing the mutant oligonucleotide primers. The basic procedure utilizes a supercoiled double-stranded DNA (dsDNA) vector with an insert of interest and two synthetic oligonucleotide primers containing the desired mutation (see Figure 1). The oligonucleotide primers, each complementary to opposite strands of the vector, are extended during temperature cycling by using PfuTurbo DNA polymerase. Incorporation of the oligonucleotide primers generates a mutated plasmid containing staggered nicks. Following temperature cycling, the product is treated with Dpn I. The Dpn I endonuclease (target sequence: 5´-Gm6ATC- 3´) is specific for methylated and hemimethylated DNA and is used to digest the parental DNA template and to select for mutation-containing synthesized DNA.6 DNA isolated from almost all E. coli strains is dam methylated and therefore susceptible to Dpn I digestion. The nicked vector DNA incorporating the desired mutations is then transformed into XL10-Gold*** Ultracompetent Cells. The small amount of starting DNA template required to perform this method, the high-fidelity of the PfuTurbo DNA polymerase, and the low number of thermal cycles all contribute to the high mutation efficiency and decreased potential for random mutations.
Note While plasmid DNA isolated from almost all of the commonly used E. coli strains (dam+) is methylated and is a suitable template for mutagenesis, plasmid DNA isolated from the exceptional dam–
E. coli strains, including JM110 and SCS110, is not suitable.
* U.S. Patent Nos. 5,789,166, 5,932,419, 6,391,548, 6,713,285, 7,132,265, 7,176,004,
5,286,632 and patents pending. ** U.S. Patent Nos. 5,545,552, 5,866,395, 5,948,663, 6,183,997, 6,444,428, 6,489,150,
6,734,293, 7,045,328, and patents pending. ll PfuTurbo DNA polymerase has 6-fold higher fidelity in DNA synthesis than Taq DNA
polymerase. *** U.S. Patent Nos. 5,512,468 , 5,707,841, 6,706,525, and patents pending and equivalent
foreign patents.
FIGURE 1 Overview of the QuikChange XL site-directed mutagenesis method.
The QuikChange XL site-directed mutagenesis kit is a specialized version of our popular QuikChange site-directed mutagenesis kit, created for efficient mutagenesis of large or otherwise difficult-to-mutagenize plasmid templates. The QuikChange XL kit features components specifically designed for more efficient DNA replication and bacterial transformation. The QuikChange solution is provided to facilitate replication of large plasmids, while XL10-Gold ultracompetent cells have been included to ensure the highest transformation efficiencies possible. The transformation efficiency of XL10-Gold cells is 5-fold higher than the transformation efficiency of XL1-Blue cells employed in the original QuikChange kit.7 Moreover, XL10-Gold cells contain the Hte phenotype, which increases the transformation efficiency of larger DNA plasmids.
QUIKCHANGE XL MUTAGENESIS CONTROL To demonstrate the effectiveness of the QuikChange XL method, the pWhitescript 4.5-kb control plasmid is used to test the efficiency of mutant plasmid generation. The pWhitescript 4.5-kb control plasmid contains a stop codon (TAA) at the position where a glutamine codon (CAA) would normally appear in the β-galactosidase gene of the pBluescript II SK(–) phagemid (corresponding to amino acid 9 of the protein). XL10-Gold ultracompetent cells transformed with this control plasmid appear white on LB–ampicillin agar plates (see Preparation of Media and Reagents), containing IPTG and X-gal, because β-galactosidase activity has been obliterated. The oligonucleotide control primers create a point mutation that reverts the T residue of the stop codon (TAA) in the β-galactosidase gene encoded on the pWhitescript 4.5-kb control template to a C residue to produce a glutamine codon (Gln, CAA). Following transformation, colonies can be screened for β-galactosidase production (β-gal+) by virtue of a blue colony phenotype.
MUTAGENIC PRIMER DESIGN
Note Mutagenic primers can be designed using our web-based QuikChange Primer Design Program available online at www.agilent.com/genomics/qcpd.
Primer Design Guidelines The mutagenic oligonucleotide primers for used with this protocol must be designed individually according to the desired mutation. The following considerations should be made for designing mutagenic primers:
♦ Both mutagenic primers must contain the desired mutation and anneal to the same sequence on opposite strands of the plasmid.
♦ Primers should be between 25 and 45 bases in length, with a melting temperature (Tm) of ≥78°C. Primers longer than 45 bases may be used, but using longer primers increases the likelihood of secondary structure formation, which may affect the efficiency of the mutagenesis reaction. The following formula is commonly used for estimating the Tm of primers:
mismatch % )(675/ 0.41(%GC) + 81.5 m −−= NT
For calculating Tm:
• values for %GC and % mismatch are whole numbers
For calculating Tm for primers intended to introduce insertions or deletions, use this modified version of the above formula:
)(675/ 0.41(%GC) + 81.5 m NT −=
where N does not include the bases which are being inserted or deleted.
Note When using primer design software for QuikChange site- directed mutagenesis applications, be aware that the Tm calculated by the primer design software may differ from the Tm value calculated using the formula presented above. We recommend verifying primer Tm’s using the formula above or by using the QuikChange Tm calculator, available online at www.genomics.agilent.com.
♦ The desired mutation (deletion or insertion) should be in the middle of the primer with ~10–15 bases of correct sequence on both sides.
♦ The primers optimally should have a minimum GC content of 40% and should terminate in one or more C or G bases.
Additional Primer Considerations
♦ The mutagenesis protocol uses 125 ng of each oligonucleotide primer. To convert nanograms to picomoles of oligo, use the following equation:
For example, for 125 ng of a 25-mer:
♦ Primers need not be 5´ phosphorylated but must be purified either by fast polynucleotide liquid chromatography (FPLC) or by polyacrylamide gel electrophoresis (PAGE). Failure to purify the primers results in a significant decrease in mutation efficiency.
♦ It is important to keep primer concentration in excess. We suggest that you vary the amount of template while keeping the concentration of the primer constantly in excess.
1000 oligoin bases of# 330
oligo of ng = oligo of pmoles × ×
X
×
XL10-GOLD ULTRACOMPETENT CELLS XL10-Gold ultracompetent cells are derived from the highest-efficiency Stratagene competent cell line, XL2-Blue MRF´. These strains possess the Hte phenotype, which increases transformation efficiency of ligated DNA.7 XL10-Gold cells are both endonuclease deficient (endA1) and recombination deficient (recA). The endA1 mutation greatly improves the quality of plasmid miniprep DNA,8 and the recA mutation helps ensure insert stability. In addition, the McrA, McrCB, McrF, Mrr, and HsdR systems have been removed from XL10-Gold ultracompetent cells. The mcrA, mcrCB and mrr mutations prevent cleavage of cloned DNA that carries cytosine and/or adenine methylation, which is often present in eukaryotic DNA and cDNA.9, 10, 11 The McrA and McrCB systems recognize and restrict methylated cytosine DNA sequences, and the Mrr system recognizes and restricts methylated adenine DNA sequences. The Mrr system also restricts methylated cytosine DNA sequences with a specificity differing from that of McrA and McrCB. This activity has been named McrF. This McrF activity against methylated cytosines has been shown to be equal to or greater than the restriction activity of the McrA and McrCB systems.12 The hsdR mutation prevents the cleavage of cloned DNA by the EcoK (hsdR) endonuclease system. XL10-Gold cells grow faster than XL1 or XL2-Blue cells, resulting in larger colonies. To permit blue-white color screening, the XL10-Gold ultracompetent cells contain the lacIqZΔM15 gene on the F´ episome.
Host strain References Genotype
XL10-Gold ultracompetent cells
7, 13, 14 TetR Δ(mcrA)183 Δ(mcrCB-hsdSMR-mrr)173 endA1 supE44 thi-1 recA1 gyrA96 relA1 lac Hte [F´ proAB lacIqZΔM15 Tn10 (TetR) Amy CamR]
It is important to store the XL10-Gold ultracompetent cells at –80°C to prevent a loss of efficiency. For best results, please follow the directions outlined in the following sections.
PROTOCOL
QuikSolution QuikSolution has been shown to improve linear amplification. Enhanced amplification efficiencies are observed when using between 2.5–3.5 μl QuikSolution/50 μl reaction, with 3 μl being optimal for most targets.
Mutant Strand Synthesis Reaction (Thermal Cycling)
Notes Ensure that the plasmid DNA template is isolated from a dam+ E. coli strain. The majority of the commonly used E. coli strains are dam+. Plasmid DNA isolated from dam– strains (e.g. JM110 and SCS110) is not suitable.
To maximize temperature-cycling performance, we strongly recommend using thin-walled tubes, which ensure ideal contact with the temperature cycler’s heat blocks. The following protocols were optimized using thin-walled tubes.
1. Synthesize two complimentary oligonucleotides containing the desired mutation, flanked by unmodified nucleotide sequence. Purify these oligonucleotide primers prior to use in the following steps (see Mutagenic Primer Design).
2. Prepare the control reaction as indicated below:
5 μl of 10× reaction buffer (see Preparation of Media and Reagents) 2 μl (10 ng) of pWhitescript 4.5-kb control plasmid (5 ng/μl) 1.25 μl (125 ng) of oligonucleotide control primer #1
[34-mer (100 ng/μl)] 1.25 μl (125 ng) of oligonucleotide control primer #2
[34-mer (100 ng/μl)] 1 μl of dNTP mix 3 μl of QuikSolution 36.5 μl of double-distilled water (ddH2O) to a final volume of 50 μl
Then add
3. Prepare the sample reaction(s) as indicated below:
Note Set up an initial sample reaction using 10 ng of dsDNA template. If this initial reaction is unsuccessful, set up a series of sample reactions using various concentrations of dsDNA template ranging from 5 to 50 ng (e.g., 5, 10, 20, and 50 ng of dsDNA template) while keeping the primer concentration constant.
5 μl of 10× reaction buffer X μl (10 ng) of dsDNA template X μl (125 ng) of oligonucleotide primer #1 X μl (125 ng) of oligonucleotide primer #2 1 μl of dNTP mix 3 μl of QuikSolution ddH2O to a final volume of 50 μl
Then add
1 μl of PfuTurbo DNA polymerase (2.5 U/μl)
4. If the thermal cycler to be used does not have a hot-top assembly, overlay each reaction with ~30 μl of mineral oil.
5. Cycle each reaction using the cycling parameters outlined in Table I.
Note It is important to adhere to the 18-cycle limit when cycling the mutagenesis reactions. More that 18 cycles can have deleterious effects on the reaction efficiency.
6. Following temperature cycling, place the reaction tubes on ice for 2 minutes to cool the reactions to ≤37°C.
Note If desired, amplification may be checked by electrophoresis of 10 µl of the product on a 1% agarose gel. A band may or may not be visualized at this stage. In either case proceed with Dpn I digestion and transformation.
TABLE I
Segment Cycles Temperature Time
95°C 50 seconds
60°C 50 seconds
3 1 68°C 7 minutes
* For example, a 5-kb plasmid requires 5 minutes at 68°C per cycle.
Dpn I Digestion of the Amplification Products
Note It is important to insert the pipet tip below the mineral oil overlay (if used) when adding the Dpn I restriction enzyme to the reaction tubes during the digestion step and when removing the 1 μl of the Dpn I-treated DNA for transfer to the transformation reaction. Using specialized aerosol-resistant pipet tips, which are small and pointed, will facilitate this process.
1. Add 1 μl of the Dpn I restriction enzyme (10 U/μl) directly to each amplification reaction below the mineral oil overlay using a small, pointed pipet tip.
2. Gently and thoroughly mix each reaction mixture by pipetting the solution up and down several times. Spin down the reaction mixtures in a microcentrifuge for 1 minute, then immediately incubate the reactions at 37°C for 1 hour to digest the parental (i.e., the nonmutated) supercoiled dsDNA.
Transformation of XL10-Gold Ultracompetent Cells
Notes Please read the Transformation Guidelines before proceeding with the transformation protocol.
XL10-Gold cells are resistant to tetracycline and chloramphenicol. If the mutagenized plasmid contains only the tetR or camR resistance marker, an alternative strain of competent cells must be used.
1. Gently thaw the XL10-Gold ultracompetent cells on ice. For each control and sample reaction to be transformed, aliquot 45 μl of the ultracompetent cells to a prechilled 14-ml BD Falcon polypropylene round-bottom tube.
2. Add 2 μl of the β-ME mix provided with the kit to the 45 μl of cells. (Using an alternative source of β-ME may reduce transformation efficiency.)
3. Swirl the contents of the tube gently. Incubate the cells on ice for 10 minutes, swirling gently every 2 minutes.
4. Transfer 2 μl of the Dpn I-treated DNA from each control and sample reaction to separate aliquots of the ultracompetent cells.
Note Carefully remove any residual mineral oil from the pipet tip before transferring the Dpn I-treated DNA to the transformation reaction.
As an optional control, verify the transformation efficiency of the XL10-Gold ultracompetent cells by adding 1 μl of 0.01 ng/μl pUC18 control plasmid (dilute the control provided 1:10 in high-quality water) to another 45-μl aliquot of cells.
Swirl the transformation reactions gently to mix and incubate the reactions on ice for 30 minutes.
5. Preheat NZY+ broth (see Preparation of Media and Reagents) in a 42°C water bath for use in step 8.
Note Transformation of XL10-Gold ultracompetent cells has been optimized using NZY+ broth.
6. Heat-pulse the tubes in a 42°C water bath for 30 seconds. The duration of the heat pulse is critical for obtaining the highest efficiencies. Do not exceed 42°C.
Note This heat pulse has been optimized for transformation in 14-ml BD Falcon polypropylene round-bottom tubes.
7. Incubate the tubes on ice for 2 minutes.
8. Add 0.5 ml of preheated (42°C) NZY+ broth to each tube, then incubate the tubes at 37°C for 1 hour with shaking at 225–250 rpm.
9. Plate the appropriate volume of each transformation reaction, as indicated in the table below, on agar plates containing the appropriate antibiotic for the plasmid vector.
For the mutagenesis and transformation controls, spread cells on LB–ampicillin agar plates containing 80 μg/ml X-gal and 20 mM IPTG (see Preparing the Agar Plates for Color Screening).
Transformation reaction plating volumes
Reaction Type Volume to Plate
pWhitescript mutagenesis control 250 μl
pUC18 transformation control 5 μl (in 200 μl of NZY+ broth)*
Sample mutagenesis 250 μl on each of two plates (entire transformation reaction)
* Place a 200-μl pool of NZY+ broth on the agar plate, pipet the 5 μl of the transformation reaction into the pool, then spread the mixture.
10. Incubate the transformation plates at 37°C for >16 hours.
Expected Results for the Control Transformations The expected colony number from the transformation of the pWhitescript 4.5 kb control mutagenesis reaction is between 50 and 800 colonies. Greater than 80% of the colonies should contain the mutation and appear as blue colonies on agar plates containing IPTG and X-gal.
Note The mutagenesis efficiency (ME) for the pWhitescript 4.5-kb control plasmid is calculated by the following formula:
ME Number of blue colony forming units (cfu) Total number of colony forming units (cfu)
= × 100%
If transformation of the pUC18 control plasmid was performed, >100 colonies (>109 cfu/μg) should be observed, with >98% having the blue phenotype.
Expected Results for Sample Transformations The expected colony number is between 10 and 1000 colonies, depending upon the base composition and length of the DNA template employed. For suggestions on increasing colony number, see Troubleshooting. The insert of interest should be sequenced to verify that selected clones contain the desired mutation(s).
TRANSFORMATION GUIDELINES
Storage Conditions Ultracompetent cells are sensitive to even small variations in temperature and must be stored at the bottom of a –80°C freezer. Transferring tubes from one freezer to another may result in a loss of efficiency. Ultracompetent cells should be placed at –80°C directly from the dry ice shipping container.
Aliquoting Cells When aliquoting, keep ultracompetent cells on ice at all times. It is essential that the BD Falcon polypropylene tubes are placed on ice before the cells are thawed and that the cells are aliquoted directly into the prechilled tubes.
Use of 14-ml BD Falcon Polypropylene Round-Bottom Tubes It is important that 14-ml BD Falcon polypropylene round-bottom tubes (BD Biosciences Catalog #352059) are used for the transformation protocol, since other tubes may be degraded by the β-mercaptoethanol used in the Transformation Protocol. In addition, the duration of the heat-pulse step is critical and has been optimized specifically for the thickness and shape of these tubes.
Use of β-Mercaptoethanol β-Mercaptoethanol (β-ME) has been shown to increase transformation efficiency. The XL10-Gold β-mercaptoethanol mix provided in this kit is diluted and ready to use.
Quantity of DNA Added Greatest efficiencies are observed when adding 2 μl of the ligation mixture. A greater number of colonies will be obtained when adding up to 50 ng, although the overall efficiency may be lower.
Length and Temperature of the Heat Pulse There is a defined window of highest efficiency resulting from the heat pulse during transformation. Optimal efficiencies are observed when cells are heat-pulsed for 30 seconds. Heat-pulsing for at least 30 seconds is recommended to allow for slight variations in the length of incubation. Efficiencies decrease when incubating for <30 seconds or for >40 seconds. Do not exceed 42°C.
Preparing the Agar Plates for Color Screening To prepare the LB agar plates for blue–white color screening, add 80 μg/ml of 5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside (X-gal), 20 mM isopropyl-1-thio-β-D-galactopyranoside (IPTG), and the appropriate antibiotic to the LB agar. Alternatively, 100 μl of 10 mM IPTG and 100 μl of 2% X-gal can be spread on the LB agar plates 30 minutes prior to plating the transformations. Prepare the IPTG in sterile dH2O; prepare the X-gal in dimethylformamide (DMF). Do not mix the IPTG and X-gal before pipetting them onto the plates because these chemicals may precipitate.
TROUBLESHOOTING When used according to the guidelines outlined in this instruction manual, this kit provides a reliable means to conduct site-directed mutagenesis using dsDNA templates. Variations in the base composition and length of the DNA template and in thermal cycler performance may contribute to differences in mutagenesis efficiency. We provide the following guidelines for troubleshooting these variations.
Observation Suggestion(s)
Ensure that sufficient DNA template is used in the reaction. Visualize the DNA template on a gel to verify the quantity and quality. Repeat reaction using higher amounts of plasmid DNA (100 ng, 200 ng, 500 ng).
Ensure that sufficient mutant DNA is synthesized in the reaction.
• Titrate QuikSolution in 1-μl increments from 0 to 5 μl
• Increase the amount of the Dpn I-treated DNA used in the transformation reaction to 4 μl
• Increase the extension time to 2.5 min/kb
• Precipitate the entire reaction and use all of it in the transformation
Ensure sufficient mutant DNA is synthesized by adjusting the cycling parameters for the sample reaction to overcome differences in ramping efficiencies of thermal cyclers. Increase initial denaturation step (segment 1) to 1–2 minutes and denaturation cycles (segment 2) to 1 minute.
Ensure that excess mineral oil is not transferred into the transformation reaction when pipetting the Dpn I-treated DNA. Using the smallest pipet tips available, insert the pipet tip completely below the mineral layer overlay and clear the pipet tip while submerged beneath the mineral oil overlay before collecting the sample.
Low transformation efficiency or low colony number
Ethanol precipitate the Dpn I digested PCR product, and resuspend in a decreased volume of water before transformation. Different thermal cyclers contribute to variations in cycling efficiencies. Optimize the cycling parameters (including ramp rates) for the control reaction then repeat the protocol for the sample reactions using the optimized conditions.
Ensure that ultracompetent cells are stored at the bottom of a –80°C freezer immediately upon arrival; use XL10-Gold β-ME in the transformation reactions (see also Transformation Guidelines).
Verify that the agar plates were prepared correctly. See Preparing the Agar Plates for Color Screening, and follow the recommendations for IPTG and X-Gal concentrations carefully.
For best visualization of the blue (β-gal+) phenotype, the control plates must be incubated for at least 16 hours at 37°C.
Low mutagenesis efficiency or low colony number with the control reaction
Avoid multiple freeze-thaw cycles for the dNTP mix. Thaw the dNTP mix once, prepare single-use aliquots, and store the aliquots at –20°C. Do not subject the dNTP mix to multiple freeze-thaw cycles.
Add the Dpn I restriction enzyme below the mineral oil overlay in the digestion step and ensure proper mixing of all components, especially the Dpn I, in the reaction.
Allow sufficient time for the Dpn I to completely digest the parental template; repeat the digestion if too much DNA template was present. Increase digestion time to 1.5–2.0 hours.
Avoid multiple freeze-thaw cycles for the dNTP mix. Thaw the dNTP mix once, prepare single-use aliquots, and store the aliquots at –20°C. Do not subject the dNTP mix to multiple freeze-thaw cycles.
Low mutagenesis efficiency with the sample reaction(s)
The formation of secondary structures may be inhibiting the mutagenesis reaction. Increasing the annealing temperature up to 68°C may help to alleviate secondary structure formation and improve mutagenesis efficiency.
Table continues on the following page
Table continues from the previous page
Poor quality primers can lead to false positives. Radiolabel the primers and check for degradation on an acrylamide gel or resynthesize the primers.
False positives
False priming can lead to false positives. Increase the stringency of the reaction by increasing the annealing temperature up to 68°C.
Unwanted deletion or recombination of plasmid DNA following mutagenesis and transformation
Transform the mutagenesis reaction into competent cells that are designed to prevent recombination events, such as Stratagene SURE 2 Supercompetent Cells (Catalog #200152). Note that SURE 2 competent cells are not recommended for use with mutagenized plasmids greater than 10 kb in size; note also that SURE 2 cells are Kanr, Tetr, and Chlr, and are not compatible with plasmid selection using kanamycin, tetracycline, or chloramphenicol resistance markers.
PREPARATION OF MEDIA AND REAGENTS
LB Agar (per Liter) 10 g of NaCl 10 g of tryptone 5 g of yeast extract 20 g of agar Add deionized H2O to a final volume of
1 liter Adjust pH to 7.0 with 5 N NaOH Autoclave Pour into petri dishes
(~25 ml/100-mm plate)
LB–Ampicillin Agar (per Liter) 1 liter of LB agar, autoclaved Cool to 55°C Add 10 ml of 10-mg/ml filter-sterilized
ampicillin Pour into petri dishes
(~25 ml/100-mm plate)
10× Reaction Buffer 100 mM KCl 100 mM(NH4)2SO4 200 mM Tris-HCl (pH 8.8) 20 mM MgSO4 1% Triton® X-100 1 mg/ml nuclease-free bovine serum
albumin (BSA)
NZY+ Broth (per Liter) 10 g of NZ amine (casein hydrolysate) 5 g of yeast extract 5 g of NaCl Add deionized H2O to a final volume
of 1 liter Adjust to pH 7.5 using NaOH Autoclave Add the following filer-sterilized
supplements prior to use: 12.5 ml of 1 M MgCl2 12.5 ml of 1 M MgSO4 20 ml of 20% (w/v) glucose (or 10 ml
of 2 M glucose)
TE Buffer 10 mM Tris-HCl (pH 7.5) 1 mM EDTA
REFERENCES 1. Kunkel, T. A. (1985) Proc Natl Acad Sci U S A 82(2):488-92. 2. Sugimoto, M., Esaki, N., Tanaka, H. and Soda, K. (1989) Anal Biochem 179(2):309-
11. 3. Taylor, J. W., Ott, J. and Eckstein, F. (1985) Nucleic Acids Res 13(24):8765-85. 4. Vandeyar, M. A., Weiner, M. P., Hutton, C. J. and Batt, C. A. (1988) Gene 65(1):129-
33. 5. Papworth, C., Bauer, J. C., Braman, J. and Wright, D. A. (1996) Strategies 9(3):3–4. 6. Nelson, M. and McClelland, M. (1992) Methods Enzymol 216:279-303. 7. Jerpseth, B., Callahan, M. and Greener, A. (1997) Strategies 10(2):37–38. 8. Wnendt, S. (1994) Biotechniques 17(2):270, 272. 9. Kohler, S. W., Provost, G. S., Kretz, P. L., Dycaico, M. J., Sorge, J. A. et al. (1990)
Nucleic Acids Res 18(10):3007-13. 10. Kretz, P. L., Kohler, S. W. and Short, J. M. (1991) J Bacteriol 173(15):4707-16. 11. Raleigh, E. A. and Wilson, G. (1986) Proc Natl Acad Sci U S A 83(23):9070-4. 12. Jerpseth, B., Greener, A., Short, J. M., Viola, J. and Kretz, P. L. (1992) Strategies
5(3):81–83. 13. Bullock, W. O., Fernandez, J. M. and Short, J. M. (1987) Biotechniques 5(4):376–378. 14. Greener, A. and Jerpseth, B. (1993) Strategies 6(2):57.
ENDNOTES Triton® is a registered trademark of Rohm and Haas Co.
MSDS INFORMATION The Material Safety Data Sheet (MSDS) information for Stratagene products is provided on the web at http://www.genomics.agilent.com. MSDS documents are not included with product shipments.
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QUICK-REFERENCE PROTOCOL ♦ Prepare the control and sample reaction(s) as indicated below:
Note Set up an initial sample reaction using 10 ng of dsDNA template. If this initial sample reaction is unsuccessful, set up a series of reactions using various concentrations of dsDNA template ranging from 5 to 50 ng (e.g., 5, 10, 20, and 50 ng of dsDNA template) while keeping the primer concentration constant.
Control Reaction 5 μl of 10× reaction buffer 2 μl (10 ng) of pWhitescript 4.5-kb control
template (5 ng/μl) 1.25 μl (125 ng) of oligonucleotide control
primer #1 [34-mer (100 ng/μl)] 1.25 μl (125 ng) of oligonucleotide control
primer #2 [34-mer (100 ng/μl)] 1 μl of dNTP mix 3 μl of QuikSolution 36.5 μl ddH2O to a final volume of 50 μl
Sample Reaction 5 μl of 10× reaction buffer X μl (10 ng) of dsDNA template X μl (125 ng) of oligonucleotide primer #1 X μl (125 ng) of oligonucleotide primer #2 1 μl of dNTP mix 3 μl of QuikSolution ddH2O to a final volume of 50 μl
♦ Then add 1 μl of PfuTurbo DNA polymerase (2.5 U/μl) to each control and sample reaction.
♦ If the thermal cycler to be used does not have a hot top assembly, overlay each reaction with ~30 μl of mineral oil.
♦ Cycle each reaction using the cycling parameters outlined in the following table:
Segment Cycles Temperature Time
95°C 50 seconds
60°C 50 seconds
3 1 68°C 7 minutes
♦ Add 1 μl of Dpn I restriction enzyme (10 U/μl) below the mineral oil overlay.
♦ Gently and thoroughly mix each reaction, spin down in a microcentrifuge for 1 minute, and immediately incubate at 37°C for 1 hour to digest the parental supercoiled dsDNA.
♦ Transform 2 μl of the Dpn I-treated DNA from each control and sample reaction into separate 45-μl aliquots of XL10-Gold ultracompetent cells (see Transformation of XL10-Gold Ultracompetent Cells in the instruction manual).
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<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> /ENU (Use these settings to create Adobe PDF documents best suited for high-quality prepress printing. Created PDF documents can be opened with Acrobat and Adobe Reader 5.0 and later.) >> /Namespace [ (Adobe) (Common) (1.0) ] /OtherNamespaces [ << /AsReaderSpreads false /CropImagesToFrames true /ErrorControl /WarnAndContinue /FlattenerIgnoreSpreadOverrides false /IncludeGuidesGrids false /IncludeNonPrinting false /IncludeSlug false /Namespace [ (Adobe) (InDesign) (4.0) ] /OmitPlacedBitmaps false /OmitPlacedEPS false /OmitPlacedPDF false /SimulateOverprint /Legacy >> << /AddBleedMarks false /AddColorBars false /AddCropMarks false /AddPageInfo false /AddRegMarks false /ConvertColors /ConvertToCMYK /DestinationProfileName () /DestinationProfileSelector /DocumentCMYK /Downsample16BitImages true /FlattenerPreset << /PresetSelector /MediumResolution >> /FormElements false /GenerateStructure false /IncludeBookmarks false /IncludeHyperlinks false /IncludeInteractive false /IncludeLayers false /IncludeProfiles false /MultimediaHandling /UseObjectSettings /Namespace [ (Adobe) (CreativeSuite) (2.0) ] /PDFXOutputIntentProfileSelector /DocumentCMYK /PreserveEditing true /UntaggedCMYKHandling /LeaveUntagged /UntaggedRGBHandling /UseDocumentProfile /UseDocumentBleed false >> ] >> setdistillerparams << /HWResolution [2400 2400] /PageSize [612.000 792.000] >> setpagedevice

manual: quikchange xl site-directed mutatgenesis kit

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